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Results: 1 to 13 of 13

Tests names and labsConditionsGenes, analytes, and microbesMethods

Abnormal mineralization disorders Deletion/ Duplication Panel

HNL Genomics Connective Tissue Gene Tests
United States
215
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Abnormal mineralization disorders Comprehensive Panel

HNL Genomics Connective Tissue Gene Tests
United States
215
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Abnormal mineralization disorders Deletion/ Duplication Panel

HNL Genomics Connective Tissue Gene Tests
United States
215
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Abnormal mineralization disorders Comprehensive Panel

HNL Genomics Connective Tissue Gene Tests
United States
215
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hypomagnesemia NGS Panel

Fulgent Genetics
United States
12123
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Primary Immunodeficiency NGS Panel

Fulgent Genetics
United States
1048472
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neuronal Migration Disorders NGS Panel

Fulgent Genetics
United States
39283
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypoparathyroidism panel

Genetic Services Laboratory University of Chicago
United States
2117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HIRA Single Gene

Fulgent Genetics
United States
851
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ARVCF Single Gene

Fulgent Genetics
United States
851
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FAT4 Single Gene

Fulgent Genetics
United States
911
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FAM111A Single Gene

Fulgent Genetics
United States
901
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 13 of 13

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.